Literature DB >> 2499293

The use of porcine factor VIII concentrate (Hyate:C) in the treatment of patients with inhibitor antibodies to factor VIII. A multicenter US experience.

D B Brettler1, A D Forsberg, P H Levine, L M Aledort, M W Hilgartner, C K Kasper, J M Lusher, C McMillan, H Roberts.   

Abstract

The response to a highly purified concentrate of porcine factor VIII was evaluated in 45 bleeding episodes in 38 patients with high responding inhibitor antibodies to factor VIII. A total of 437 infusions were given. The patients came from 25 hemophilia centers in the United States. The majority had a life- or limb-threatening hemorrhage for which other modalities had not been successful. In 32 of 45 episodes, a good to excellent response was obtained. Adverse reactions were minimal, occurring in 17 treatment episodes, and were mostly treated with antihistamines and/or hydrocortisone. No clear predictor of clinical response to porcine factor VIII concentrate was identified, including pretreatment human and porcine inhibitor levels, percentage of cross-reactivity between the human and porcine antibodies, and the presence of measurable levels of factor VIII after the porcine factor concentrate was given. Anamnesis to porcine factor VIII did occur in some instances. Porcine factor VIII is a valuable modality in the treatment of serious hemorrhages in patients with inhibitors to factor VIII. Its use should be considered early in the course of severe hemorrhage in these patients.

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Year:  1989        PMID: 2499293

Source DB:  PubMed          Journal:  Arch Intern Med        ISSN: 0003-9926


  10 in total

Review 1.  Hemophilia treatment in historical perspective: a review of medical and social developments.

Authors:  F R Rosendaal; C Smit; E Briët
Journal:  Ann Hematol       Date:  1991-02       Impact factor: 3.673

2.  Acquired hemophilia in a patient with myeloma.

Authors:  L S Loftus; W N Arnold
Journal:  West J Med       Date:  1994-02

3.  Phenotypic and genotypic stability of multiple lines of transgenic pigs expressing recombinant human protein C.

Authors:  K E Van Cott; H Lubon; C G Russell; S P Butler; F C Gwazdauskas; J Knight; W N Drohan; W H Velander
Journal:  Transgenic Res       Date:  1997-05       Impact factor: 2.788

Review 4.  Haemophilia.

Authors:  M R Cahill; B T Colvin
Journal:  Postgrad Med J       Date:  1997-04       Impact factor: 2.401

5.  Recombinant porcine factor VIII for high-risk surgery in paediatric congenital haemophilia A with high-titre inhibitor.

Authors:  S E Croteau; Y L Abajas; A S Wolberg; B I Nielsen; G R Marx; C W Baird; E J Neufeld; P E Monahan
Journal:  Haemophilia       Date:  2017-01-25       Impact factor: 4.287

Review 6.  Modern treatment of haemophilia.

Authors:  E Berntorp; V Boulyjenkov; D Brettler; M Chandy; P Jones; C Lee; J Lusher; P Mannucci; I Peak; K Rickard
Journal:  Bull World Health Organ       Date:  1995       Impact factor: 9.408

7.  Hemophilia and von Willebrand's disease: 2. Management. Association of Hemophilia Clinic Directors of Canada.

Authors: 
Journal:  CMAJ       Date:  1995-07-15       Impact factor: 8.262

Review 8.  Factor VIII inhibitors: risk factors and methods for prevention and immune modulation.

Authors:  Ai Hong Zhang; Jonathan Skupsky; David W Scott
Journal:  Clin Rev Allergy Immunol       Date:  2009-10       Impact factor: 8.667

Review 9.  Current difficulties and recent advances in bypass therapy for the management of hemophilia with inhibitors: a new and practical formulation of recombinant factor VIIa.

Authors:  Linda Butros; Koh Boayue; Prasad Mathew
Journal:  Drug Des Devel Ther       Date:  2011-05-12       Impact factor: 4.162

10.  A Hematological Menace: Multiple Venous Thrombosis Complicated by Acquired Factor VIII Deficiency.

Authors:  Robin Paudel; Luis W Dominguez; Prerna Dogra; Saurav Suman; Simon Badin; Carrie Wasserman
Journal:  Am J Case Rep       Date:  2016-04-04
  10 in total

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